NIH EXAM 2 QUESTIONS WITH CORRECT
ANSWERS!!
What describes a properly designed Case Report Form (CRF)
Collects relevant data in accordance with the protocol
Allows for efficient data in accordance with the protocol
Facilitates the pooling of data across studies
**All of the above
Scientific misconduct can cause which of the following?
Make other scientists upset because they have spent time and resources to replicate manipulated
data
Damage to institutional reputations
Undermine public perception of truthfulness of science
Loss of government financial support
Jail time
All of the above
In the proposed ethical framework for clinical research, the final principle "respect for
enrolled subjects" is understood to include:
Establishing a contract between the subject and the researcher
***Monitoring the subject's welfare and protecting confidentiality of information
Keeping the financial costs of participation reasonable
Informing the subject of new information only after the study is published
What is a systematic and independent examination of trial-related activities and documents
to determine whether the evaluation trial-related activities were conducted, and the data
were recorded, analyzed, and accurately reported according to the protocol, Standard
, Operating Procedures (SOP), Good Clinical Practice (GCP), and the applicable regulatory
requirements?
Amendment
Site initiation visit
***Audit
Routine monitoring visit
Differences in health outcomes among different demographic groups are the result of the
complex interaction of several factors, including:
A - cultural and racial/ethnic identity
B- Socioeconomic and occupational trajectory
C- Biology
D- Healthcare
E- Environment and geography
F- All of the Above
***G - A, B, and E
Which of the following statements about control groups or control arms in a study is
FALSE?
Control groups can take many different forms.
The specific question being addressed in the study directs the choice of the control group or
ANSWERS!!
What describes a properly designed Case Report Form (CRF)
Collects relevant data in accordance with the protocol
Allows for efficient data in accordance with the protocol
Facilitates the pooling of data across studies
**All of the above
Scientific misconduct can cause which of the following?
Make other scientists upset because they have spent time and resources to replicate manipulated
data
Damage to institutional reputations
Undermine public perception of truthfulness of science
Loss of government financial support
Jail time
All of the above
In the proposed ethical framework for clinical research, the final principle "respect for
enrolled subjects" is understood to include:
Establishing a contract between the subject and the researcher
***Monitoring the subject's welfare and protecting confidentiality of information
Keeping the financial costs of participation reasonable
Informing the subject of new information only after the study is published
What is a systematic and independent examination of trial-related activities and documents
to determine whether the evaluation trial-related activities were conducted, and the data
were recorded, analyzed, and accurately reported according to the protocol, Standard
, Operating Procedures (SOP), Good Clinical Practice (GCP), and the applicable regulatory
requirements?
Amendment
Site initiation visit
***Audit
Routine monitoring visit
Differences in health outcomes among different demographic groups are the result of the
complex interaction of several factors, including:
A - cultural and racial/ethnic identity
B- Socioeconomic and occupational trajectory
C- Biology
D- Healthcare
E- Environment and geography
F- All of the Above
***G - A, B, and E
Which of the following statements about control groups or control arms in a study is
FALSE?
Control groups can take many different forms.
The specific question being addressed in the study directs the choice of the control group or
